Impact of ceftazidime-avibactam on mortality in bloodstream infections: a cohort study in patients with acute leukemia.

IF 3.8 Q2 INFECTIOUS DISEASES
Therapeutic Advances in Infectious Disease Pub Date : 2025-08-16 eCollection Date: 2025-01-01 DOI:10.1177/20499361251362955
Cesar Copaja-Corzo, Susy Bazán-Ruiz, Andre Fuentes-Yufra, Marlies Pizarro-Perea, Marco Montiel-González, Giancarlo Pérez-Lazo
{"title":"Impact of ceftazidime-avibactam on mortality in bloodstream infections: a cohort study in patients with acute leukemia.","authors":"Cesar Copaja-Corzo, Susy Bazán-Ruiz, Andre Fuentes-Yufra, Marlies Pizarro-Perea, Marco Montiel-González, Giancarlo Pérez-Lazo","doi":"10.1177/20499361251362955","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Bloodstream infections (BSI) caused by carbapenemase-producing <i>Enterobacterales</i> (CPE) represent a significant threat to patients with acute leukemia due to their high mortality. Ceftazidime-avibactam (CAZ-AVI) has emerged as a therapeutic alternative against these infections; however, its efficacy in immunocompromised patients remains unclear.</p><p><strong>Objective: </strong>To determine the impact of ceftazidime-avibactam on mortality due to BSI caused by CPE in patients with acute leukemia.</p><p><strong>Design: </strong>A retrospective cohort study was conducted at the Hospital Nacional Edgardo Rebagliati Martins in Lima, Peru.</p><p><strong>Methods: </strong>We included patients diagnosed with acute leukemia who developed BSI due to CPE during their hospital stays. Mortality was assessed for up to 30 days after BSI onset.</p><p><strong>Results: </strong>We evaluated 41 patients with a median age of 51 years; 56.1% had acute myeloid leukemia and 43.9% had acute lymphoblastic leukemia. Mortality at 30 days occurred in 60.9% of patients. The most frequent type of chemotherapy administered was induction (51.2%). Empiric antibiotic therapy with meropenem was administered to 97.6% of the patients, and ceftazidime-avibactam was prescribed as a targeted therapy to 48.8%. In the multivariate Cox regression model, the prescription of ceftazidime-avibactam reduced the risk of death (adjusted hazard ratio, 0.29; 95% CI: 0.09-0.92; <i>p</i> = 0.012) compared with those who received other antibiotic therapies, such as colistin.</p><p><strong>Conclusion: </strong>In patients with acute leukemia who developed bloodstream infections due to CPE during hospitalization, the prescription of ceftazidime-avibactam reduced 30-day mortality risk.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251362955"},"PeriodicalIF":3.8000,"publicationDate":"2025-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12357988/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Advances in Infectious Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20499361251362955","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Bloodstream infections (BSI) caused by carbapenemase-producing Enterobacterales (CPE) represent a significant threat to patients with acute leukemia due to their high mortality. Ceftazidime-avibactam (CAZ-AVI) has emerged as a therapeutic alternative against these infections; however, its efficacy in immunocompromised patients remains unclear.

Objective: To determine the impact of ceftazidime-avibactam on mortality due to BSI caused by CPE in patients with acute leukemia.

Design: A retrospective cohort study was conducted at the Hospital Nacional Edgardo Rebagliati Martins in Lima, Peru.

Methods: We included patients diagnosed with acute leukemia who developed BSI due to CPE during their hospital stays. Mortality was assessed for up to 30 days after BSI onset.

Results: We evaluated 41 patients with a median age of 51 years; 56.1% had acute myeloid leukemia and 43.9% had acute lymphoblastic leukemia. Mortality at 30 days occurred in 60.9% of patients. The most frequent type of chemotherapy administered was induction (51.2%). Empiric antibiotic therapy with meropenem was administered to 97.6% of the patients, and ceftazidime-avibactam was prescribed as a targeted therapy to 48.8%. In the multivariate Cox regression model, the prescription of ceftazidime-avibactam reduced the risk of death (adjusted hazard ratio, 0.29; 95% CI: 0.09-0.92; p = 0.012) compared with those who received other antibiotic therapies, such as colistin.

Conclusion: In patients with acute leukemia who developed bloodstream infections due to CPE during hospitalization, the prescription of ceftazidime-avibactam reduced 30-day mortality risk.

头孢他啶-阿维巴坦对急性白血病患者血液感染死亡率的影响
背景:产碳青霉烯酶肠杆菌(CPE)引起的血流感染(BSI)由于其高死亡率对急性白血病患者构成重大威胁。头孢他啶-阿维巴坦(CAZ-AVI)已成为治疗这些感染的替代方案;然而,其对免疫功能低下患者的疗效尚不清楚。目的:探讨头孢他啶-阿维巴坦对急性白血病CPE致BSI死亡率的影响。设计:在秘鲁利马的Edgardo Rebagliati Martins国立医院进行了一项回顾性队列研究。方法:我们纳入了诊断为急性白血病并在住院期间因CPE发生BSI的患者。在BSI发病后30天内评估死亡率。结果:我们评估了41例患者,中位年龄51岁;56.1%为急性髓性白血病,43.9%为急性淋巴细胞白血病。30天死亡率为60.9%。最常见的化疗类型是诱导化疗(51.2%)。97.6%的患者经经验使用美罗培南抗生素治疗,48.8%的患者使用头孢他啶-阿维巴坦作为靶向治疗。在多变量Cox回归模型中,与接受粘菌素等其他抗生素治疗的患者相比,头孢他啶-阿维巴坦处方降低了死亡风险(校正风险比为0.29;95% CI: 0.09-0.92; p = 0.012)。结论:急性白血病患者住院期间因CPE发生血流感染,头孢他啶-阿维巴坦处方可降低30天死亡风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书